NHC Key Laboratory of Radiobiology, School of Public Health, Jilin University, Changchun, China.
Int J Radiat Biol. 2023;99(3):384-395. doi: 10.1080/09553002.2022.2089365. Epub 2022 Jul 27.
Radiation-induced pulmonary fibrosis (RIPF) is a common and serious adverse effect of radiotherapy for thoracic tumors, which occurs in the irreversible stage of radiation-induced lung injury (RILI) >6 months after irradiation. It is characterized by progressive and irreversible destruction of lung tissue and deterioration of lung function, which may impair quality of life and lead to respiratory failure and death. We hope this will draw attention to the involvement of epigenetics in the regulation of RIPF.
This review summarizes research progress on the role and mechanism of DNA methylation, noncoding RNA and RNA methylation in RIPF or RILI, and the possible role and mechanism of histone modification in RIPF. We have noticed that in tissue fibrosis, the epigenetic regulation mechanisms inside and outside the nucleus can influence each other. We speculate that RIPF may be regulated by an epigenetic regulatory network during its development, and believe that TGF-β, SNAIL, PTEN and EZH2 are four targets worthy of in-depth study.
放射性肺纤维化(RIPF)是胸部肿瘤放疗后的一种常见且严重的不良反应,发生于照射后 >6 个月的放射性肺损伤(RILI)不可逆阶段。其特征为肺组织进行性、不可逆转的破坏和肺功能恶化,可能会降低生活质量,并导致呼吸衰竭和死亡。我们希望这将引起人们对表观遗传学在 RIPF 调控中的作用的关注。
本综述总结了 DNA 甲基化、非编码 RNA 和 RNA 甲基化在 RIPF 或 RILI 中的作用和机制,以及组蛋白修饰在 RIPF 中的可能作用和机制。我们注意到,在组织纤维化中,核内外的表观遗传调控机制可以相互影响。我们推测,在 RIPF 的发展过程中可能受到一个表观遗传调控网络的调控,并认为 TGF-β、SNAIL、PTEN 和 EZH2 是四个值得深入研究的靶点。